RS769983049 FMO3

Health Risk Chr 1:171108154
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Trimethylaminuria
Inborn genetic diseases
Trimethylaminuria
Other Variants in FMO3
rs61753344 rs72549323 rs72549326 rs72549334 rs72549325 rs72549331 rs72549330 rs72549322 rs72549332 rs72549320
Ask Dr. Hemsworth about this variant